Regulatory Affairs Leader - AI Software Devices (f/m/d)
Tasks
- Apply regulatory requirements to submissions
- Assess product changes impact
- Determine new or revised licenses registrations
- Develop regulatory strategy
- Ensure postmarket compliance
- Ensure premarket submissions compliance
- Manage notified body audits
- Optimize regulatory submission pathways
- Plan registration submissions
- Provide regulatory leadership
- Research and analyze regulatory background information
- Review advertising and promotion materials
- Support quality system audits
- Write and edit technical documents
Perks/Benefits
- N/A
Skills/Tech-stack
Advertising review | Clinical data | Medical Device | Medical device regulations | Postmarket Compliance | Premarket Compliance | Project Management | Quality System | Regulatory Submissions | Regulatory strategy | Risk Assessment | Technical documentation
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